HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 2,4,6-Trimethylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Biphenyl | HCID 7095 | — |
| Reactant | Mesitylene | HCID 7947 | — |
| Reactant | 2,4,6-Trimethylbiphenyl | HCID 19876 | — |
| Reactant | Stk331795 | HCID 10125229 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2,4,6-Trimethylphenol | HCID 10698 | 50% |
Reaction Steps
In a flask, 1.17 g (15 mmol) of benzene, 1.38 g (11 mmol) of mesitylene, 4.5 mg (0.02 mmol) of palladium(II) acetate, 323 mg (about 0.14 mmol) of H4PMo11V1O40-nH2O, and 10 ml of acetic acid were placed and were stirred at a constant temperature of 90° C. in an atmosphere of oxygen gas at 1 atm (0.1 MPa) for 15 hours. The resulting reaction mixture was analyzed by gas chromatography to find that 0.59 g (3.8 mmol) of biphenyl, 0.82 g (4.2 mmol) of 1,3,5-trimethyl-2-phenylbenzene, 0.85 g (3.6 mmol) of 1,3,5-trimethyl-2-(3′,5′-dimethylbenzyl)benzene, 0.13 g (1.4 mmol) of phenol, and 0.10 g (0.7 mmol) of 2,4,6-trimethylphenol were produced.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414160B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-1541eac1aa384f5fb243b8de672f21cb |
| Source note | uspto-grants-2008_08 |